EP2178374B1 - Procedes de lutte contre les algues a l'aide de thaxtomine et compositions de thaxtomine - Google Patents

Procedes de lutte contre les algues a l'aide de thaxtomine et compositions de thaxtomine Download PDF

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Publication number
EP2178374B1
EP2178374B1 EP08745224A EP08745224A EP2178374B1 EP 2178374 B1 EP2178374 B1 EP 2178374B1 EP 08745224 A EP08745224 A EP 08745224A EP 08745224 A EP08745224 A EP 08745224A EP 2178374 B1 EP2178374 B1 EP 2178374B1
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Prior art keywords
algae
thaxtomin
hydroxy
accordance
thaxtomins
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EP08745224A
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German (de)
English (en)
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EP2178374A2 (fr
Inventor
Yaowei Kang
Shawn Semones
Jonathan Leder
Anh Tran
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Novozymes Biologicals Inc
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Novozymes Biologicals Inc
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Priority to EP12177744.5A priority Critical patent/EP2520167B1/fr
Priority to EP14168205.4A priority patent/EP2792243B1/fr
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/60—1,4-Diazines; Hydrogenated 1,4-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
    • A01N63/20—Bacteria; Substances produced thereby or obtained therefrom
    • A01N63/28—Streptomyces

Definitions

  • This disclosure relates to inhibiting the growth of algae with one or more thaxtomins.
  • the methods are useful for application to water such as raw water, or algae contaminated surfaces or equipment in need of treatment to control, minimize and/or eliminate algae.
  • U.S. Patent No. 5,407,899 describes copper sulfate used for algae control.
  • Known algaecide agents kill the algae and return the water to a more desired appearance of clear or less colored waters.
  • known algaecides are problematic in that they may be costly and potentially toxic to the environment.
  • the use of algaecides has not necessarily altered the water conditions, which remain suitable for subsequent growth of algae, and/or renewed contamination.
  • Thaxtomins are a known group of phytotoxins, however, although thaxtomin A and analogues thereof demonstrate many of the biological properties desirable in potential herbicides, they are known to lack the systemic phytotoxicity critical to deliver reliable weed control in the field at low herbicide rates. See, for example, Herbicidal Properties of the Thaxtomin Group of Phytotoxins, J. Agric. Food Chem., Vol. 49, No. 5, 2001 . Thaxtomins are also known to inhibit cellulose synthesis in Arabidopsis (see The Plan Cell, Vol. 15, 1781-1794, August 2003 ).
  • the present disclosure provides one or more novel algaecides and methods for inhibiting the growth of algae by contacting algae with an effective amount of one or more thaxtomins and/or analogues thereof.
  • suitable thaxtomins include thaxtomin A, thaxtomin B, thaxtomin D, and combinations thereof.
  • thaxtomin A is used in accordance with the present disclosure.
  • the present methods are suitable where the algae is in a liquid environment, such as water.
  • Suitable liquid environments include pools, ponds, fish farms, lakes, streams, paddies, rivers, oceans, estuaries, freshwater aquariums, salt water aquariums, aquacultures, tanks for commercial aquaculture, ponds for commercial aquaculture, ornamental ponds, water gardens, run-off streams or ditches and combinations thereof.
  • the algae are in a soil or mud environment
  • the algae is contaminating containers, tanks, bioreactors or other apparatus used to commercially grow algae, such as algae grown for biofuel or alternative energy purposes.
  • the present disclosure relates to a method of inhibiting the growth of algae comprising, or consisting of contacting algae with an effective amount of one or more thaxtomins.
  • the one or more thaxtomins include compounds comprising, or consisting of thaxtomin A, thaxtomin B, thaxtomin D, and combinations thereof.
  • the one or more thaxtomins only include thaxtomin A.
  • the algae is in a liquid environment, such as water.
  • suitable liquid environments include a pool, pond, paddy, lake, stream, river, ocean, estuary, freshwater aquarium, salt water aquarium, tank for commercial aquaculture, pond for commercial aquaculture, ornamental pond, water garden, run-off stream, and combinations thereof.
  • the algae suitable for treatment are found in a soil or mud environment.
  • treatments include applying an effective amount of thaxtomin such as in an amount where the applied concentration is 0.5 ppm to 100 ppm.
  • the present disclosure provides a method of controlling the growth of algae comprising, or consisting of contacting algae with one or more thaxtomins.
  • one or more thaxtomins are applied to an area in need of algae control such as a bioreactor, tank, farm equipment, and combinations thereof.
  • thaxtomin is mixed with a carrier to form a solution having thaxtomin at concentration of 0.05 ppm to 500 ppm.
  • a solution can be applied to a contaminated surface in need of decontamination or algae reduction or elimination.
  • algae refers to any of various chiefly aquatic, eukaryotic, photosynthetic organisms, ranging in size from single-celled forms to the giant kelp.
  • the term may further refer to photosynthetic protists responsible for much of the photosynthesis on Earth.
  • the algae are polyphyletic. Accordingly, the term may refer to any protists considered to be algae from the following groups: alveolates, chloraraachniophytes, cryptomonads, euglenids, glaucophytes, haptophytes, red algae such as Rhodophyta, stramenopiles, and viridaeplantae.
  • the term refers to the green, yellow-green, brown, and red algae in the eukaryotes.
  • the term may also refer to the cyanobacteria in the prokaryotes.
  • the term also refers to green algae, blue algae, and red algae.
  • algaecide refers to one or more agents, compounds and/or compositions having algaestatic and/or algaecidal activity.
  • algaecidal means the killing of algae.
  • algaestatic as used herein means inhibiting the growth of algae, which can be reversible under certain conditions.
  • lower alkyl refers to branched or straight chain acyclic alkyl group including one to about eighteen carbon atoms.
  • exemplary alkyl groups include, inter alia, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, pentyl, iso-amyl, hexyl, octyl, decyl, and the like.
  • hydroxy refers to -OH.
  • H refers to a hydrogen atom
  • ppm refers to parts-per-million.
  • Streptomyces scabies, S . acidiscabies, and S. turgidiscabies are the causative agents of scab disease on a variety of underground potato.
  • a class of phytotoxins, thaxtomin have been identified therefrom which are involved in the pathogenesis. It has now been found that thaxtomins are suitable for the control, reduction, and/or elimination of algae, including green algae, blue algae, and red algae.
  • Thaxtomins have been found to have algaecidal and algaestatic activity.
  • the present disclosure provides methods and compositions for inhibiting the growth of algae.
  • the methods include applying a predetermined amount of algaecide to an area in need of control or treatment such as an algae contaminated area.
  • the algaecide may be in solution and/or solvated and made available to kill, control and/or minimize algae.
  • the algaecide is in solution, thus is available to penetrate the algae in a bio-effective form.
  • Suitable algaecides for use in accordance with this disclosure include one or more thaxtomins.
  • Thaxtomins include any of the type from a family of cyclic dipeptides, such as 4-nitroindol-3-yl-containing 2,5-dioxoperazines commonly known as the thaxtomins.
  • Suitable thaxtomins include agents described as cyclic dipeptides having the basic structure cyclo-(L-4-nitrotryptophyl-L-phenytalanyl).
  • suitable diketopiperazine moieties may be N-methylated, and include congeners carrying phenylalanyl ⁇ - and ring-carbon hydroxyl groups.
  • Non-limiting examples of suitable thaxtomins for use in accordance with the present disclosure include thaxtomin A, thaxtomin A ortho isomer, thaxtomin B, and C-14 deoxythaxtomin B (thaxtomin D). Combinations of thaxtomins and derivatives thereof are also suitable for use in accordance with the present disclosure.
  • purified thaxtomins are suitable algaecides for use in accordance with the present disclosure.
  • the chemical compositions include:
  • R 1 is methyl or H.
  • R 2 is hydroxy or H.
  • R 3 is methyl or H.
  • R 4 is hydroxy or H.
  • R 6 is hydroxy or H.
  • R 8 hydroxy or H.
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is methyl
  • R 4 is H
  • R 5 is hydroxy
  • R 6 is H.
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is methyl
  • R 4 is hydroxy
  • R 5 is H
  • R 8 is H.
  • R 1 is methyl
  • R 2 is H
  • R 3 is H
  • R 4 is H
  • R 5 is H
  • R 6 is H.
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is methyl
  • R 4 is H
  • R 5 is H
  • R 6 is H.
  • R 1 is methyl
  • R 2 is H
  • R 3 is methyl
  • R 4 is H
  • R 5 is H
  • R 6 is H.
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is H
  • R 4 is H
  • R 5 is H
  • R 6 is H.
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is methyl
  • R 4 is H
  • R 5 is H
  • R 6 is hydroxy
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is methyl
  • R 4 is H
  • R 5 is hydroxy
  • R 6 is hydroxy
  • R 1 is methyl
  • R 2 is hydroxy
  • R 3 is H
  • R 4 is H
  • R 5 is hydroxy
  • R 6 is H.
  • R 1 is H
  • R 2 is hydroxy
  • R 3 is methyl
  • R 4 is H
  • R 5 is hydroxy
  • R 6 is H.
  • R 1 is H
  • R 2 is H
  • R 3 is H
  • R 4 is H
  • R 5 is H
  • R 6 is H
  • purified thaxtomin A is a suitable algaecide for use in accordance with the present disclosure.
  • Thaxtomin A is a yellow compound composed of 4-nitroindol-3-yl-containing 2,5-dioxopiperazine and is the predominant thaxtomin produced by Streptomyces scabies, Streptomyces acidiscabies, and Streptomyces turgidiscabies, with phenylalanyl m -ring and ⁇ -C hydroxyl addition.
  • the chemical composition comprises, or consists of:
  • thaxtomin on algae is not known. However, not wishing to be bound by the present disclosure it is believed thaxtomins when contacted with algae inhibit cellulose biosynthesis.
  • unpurified supernatant from cell cultures such as cell cultures of Streptomyces scabies, Streptomyces acidiscabies, and Streptomyces turpidiscabies containing one or more thaxtomin(s) is suitable for use as an algaecide in accordance with the present disclosure
  • supernatant is readily obtainable from cell cultures, such as through centrifugation and collection of the remaining liquid portion.
  • one or more thaxtomins can be applied to algae contaminated environments to control, minimize and/or eliminate undesirable algae.
  • the word "treat,” “treating” or “treatment” refers to using the thaxtomins of the present disclosure prophytactically to prevent outbreaks of undesirable or high algae blooms, or to ameliorate an existing algae contamination. A number of different treatments are now possible, which control, reduce and/or eliminate algae.
  • algae contamination refers to any detectable algae manifestation(s) caused by one or more algae. Such manifestations can be caused by a number of factors such as, for example, water column nutrient levels, and/or other stressed or dysfunctional environmental states. Non-limiting examples of such manifestations include the development of algae growths, algae scum formation, low levels of dissolved oxygen In a water body, stress on aquatic and fish populations, and/or other forms of reduced environmental quality. It is understood, that the environmental conditions are non-limiting and that only a portion of the environmental conditions suitable for treatment in accordance with the present disclosure are listed herein. Further, algae contamination may also refer to residual algae left over on algae growing apparatuses and equipment such as those used to make algae oil for alternative energy production.
  • Non-limiting examples of equipment and various apparatus that can be cleaned in accordance with the present disclosure include items described in U.S. Patent Nos: 5,088,231 , 5,171,683 , 4,978,505 , 4,908,315 . Farm equipment and bioreactors used to grow algae for commercial purposes can be cleaned using the algaecide in accordance with the present disclosure.
  • compositions for use in accordance with the present disclosure contain one or more thaxtomins in an effective amount to improve water conditions.
  • effective amount refers to an amount of thaxtomin or compound(s) or composition(s) having thaxtomin constituents in accordance with the present disclosure sufficient to induce a particular positive benefit to environmental conditions such as water conditions or conditions considered contaminated or soiled with algae.
  • the positive benefit can be cosmetic in nature, or health-related, or a combination of the two.
  • the positive benefit is achieved by contacting a contaminated environment, area, or apparatus with one or more thaxtomins, and/or one or more thaxtomin constituents, to improve conditions such as algae bloom or algae contamination.
  • Treatments include contacting algae contaminated environments or soiled equipment with an amount of thaxtomin effective to be algaecidal and/or algaestatic.
  • thaxtomin concentration applied generally depends on the purpose for which the composition is to be applied. For example, the dosage and frequency of application can vary depending upon the type and severity of the algae condition.
  • one or more thaxtomins are applied to a water body such that the thaxtomin concentration is in an amount of 1 ppm to 5 ppm.
  • one or more thaxtomins are applied to a water body such that the thaxtomin concentration is applied in an amount of 0.5 ppm to 100 ppm.
  • thaxtomin is mixed with a carrier (such as water) in an amount of 0.05 ppm to 500 ppm and applied to a contaminated area or algae soiled equipment.
  • Treatments in accordance with the present disclosure contact algae contaminated areas and/or equipment with one or more thaxtomins in an effective amount to improve algae related conditions.
  • areas in need of treatment or algae control such as pools, ponds, paddies, fish farms, lakes, estuaries, oceans, freshwater aquariums, salt water aquariums, tanks for commercial aquaculture, ponds for commercial aquaculture, ornamental ponds, water gardens, alternative fuel manufacturing equipment or apparatuses, run-off ditches, house sidings, and deck planks are treated by applying to these areas, one or more thaxtomin compositions.
  • the active thaxtomin ingredient is applied until the treatment goals are obtained.
  • the duration of the treatment can vary depending on the severity of the condition. For example, treatments can last several days to weeks depending on whether the goal of treatment is to control, reduce and/or eliminate algae contamination.
  • thaxtomins may be combined with a solvent vehicle to make a formulation for the treatment of algae in which the major active ingredient is one or more thaxtomins.
  • the active ingredients are provided in suspensions, dry form(s), and aqueous solutions.
  • the amount of thaxtomin mixed with the solvent will vary depending on a number of factors, including, for example, the activity of thaxtomin, the type of thaxtomin selected, the ultimate form of the product and the particular disclosed solvent employed. Generally, the thaxtomin constituent will constitute from 1 to 95 weight percent of the thaxtomin/solvent mixture.
  • the thaxtomin constitutes from 10.00 to 80 weight percent of the thaxtomin/solvent mixture.
  • Solvents useful for preparing the present thaxtomin compositions include any solvent capable solubilizing one or more thaxtomins. Non-limiting examples of such solvents include water and/or aqueous solutions.
  • thaxtomins may be combined with a dry excipients to make a formulation for the treatment of algae in which the major active ingredient is one or more thaxtomins.
  • the active ingredients are provided in dry form.
  • the thaxtomin constituent will constitute from 1 to 95 weight percent of the thaxtomin dry formulation. In embodiments, the thaxtomin constitutes from 10.00 to 80 weight percent of the thaxtomin dry formulation.
  • Supernatant of Streptomyces acidiscabies is effective to control or reduce the following green algae: Oedogonium foveolatum, Spirogyra spp. Volvox aureus, Volvox globator, Closterium sp. Chlamydomonas sp. in as low as a 100 fold dilution.
  • Streptomyces acidiscabies was grown in Oat Meal Broth liquid medium at room temperature for 5 days. Cell culture was centrifuged and the supernatant was collected, filtered through a 0.45 ⁇ m filter, and saved for bioactivity assay. The supernatant was evaluated against above-mentioned algae at various dilutions. The algae were obtained from Carolina Biological Supply Company and were grown and maintained according to the supplied manual. Alga-Cro Freshwater Medium from Carolina Biological Supply Company was used for growing algae. Maximum Dilution for Inhibition (MDI) was used to measure the activity of the supernatant to algae. The assay was run for 3 weeks. Algae growth was visibly inhibited by that diluted supernatant.
  • MDI Maximum Dilution for Inhibition
  • the supernatant of Streptomyces acidiscabies was demonstrated to be toxic to blue-green algae: Blue-green algae ( Oscillatoria sp ) was obtained from Carolina Biological Supply Company and grown in a recommended medium (Alga-Cro Freshwater Medium). The supernatant of S. acidiscabies was added into the culture of Algae at various dilutions. The treated algae culture was incubated at room temperature under the regular room light. Three weeks later, algae growth was evaluated in terms of growth inhibition. The results showed the maximum dilution for inhibition for this blue-algae growth is greater than 50 fold.
  • a negative thaxtomin production mutant was obtained from Cornell University and used as a negative control. Wild type strain and the negative mutant were grown in oat bran liquid medium at 25°C and their supernatants used for bioassay against the algae in Table 3. The results are show the tested algae were greatly inhibited by the supernatant from wild type strain at more that 10 to 100 fold dilution. However, the supernatant from thaxtomin negative mutant showed no visible inhibition to the tested organisms.
  • thaxtomin Purified thaxtomin was used for a bioassay test and its efficacy evaluated and compared with copper sulphate, an active ingredient for many copper based algaecides. The bioassay was run for two weeks and inhibition of algae growth was evaluated. The results are in the table below. It was concluded that as low as 1ppm of purified thaxtomin was effective to control, and kill the tested algae. However 2 ppm of cupper sulfate (commercial recommended rate for cupper sulfate) was not very effective against the tested organisms in our assay system. Table 4: Bioactivity of purified thaxtomin verse CuSO4 Tested organisms Thaxtomin (1ppm) CuSO4(2ppm) Oedogonium spp.
  • Thaxtomin was effective to control algae in a minipond ecosystem.
  • a minipond ecosystem was obtained from Carolina Biological Supply Company (13-1207).
  • the system included an algae mixture ( Oedogonium, Volvox, Chlamydomonas ) and a protozoan mixture ( Amoeba, Paramecium, Euglena, Stentor, Volvox, and Chilomonas ).
  • the minipond ecosystems were set up based on the supplied manual.
  • a 20 fold dilution of fermented thaxtomin supernatant was applied to the pond system.
  • a 2 ppm CuSO4 solution and water were applied to identical systems as positive control and negative control respectively.
  • Thaxtomin was demonstrated to possess very high activity at low concentration in controlling the growth of a wide variety of algae. Thaxtomin was added to water and algae in a test tube. Table 6 Constituents Prior to Treatment-Characteristics of water and algae mix Results (after contact with thaxtomin) Control Group 2 ml water and algae (mix) Distinct bright green algae. No change, distinct bright green algae suspended in solution. Treatment 1 Thaxtomin was added to 2 m water and algae mix (thaxtomin concentration 0.5 ppm) Distinct bright green algae. Significant changes including the reduction in visible algae in solution. Algae killed resulting in appearance of yellow and brown colored (dead) algae. A 10 fold reduction in algae is observed. Some green algae was still present in the solution. Treatment 2 10mMol (2,840 ppm) of Metolachlor was applied to 2 ml water and algae mix. Distinct bright green algae. No change, distinct bright green algae suspended in solution.
  • Metolachlor (2-chloro- N -(6-ethyl-o-tolyl)- N -[(1 RS )-2-methoxy-1-methylethyl]acetamide) is a known pre-emergent herbicide commonly used to control annual grasses and some broadleaves such as Eastern black nightshade and pigweeds. At concentrations effective in terrestrial weed control (10mMol), Metolachlor did not show any algaestatic and/or algaecidal activity. Conversely, thaxtomin was very effective in controlling green algae at a dose of only 0.5 ppm, much lower than the concentration needed to control terrestrial weeds (5-10ppm).
  • Thaxtomin was show to possess very high activity at low concentration in controlling the growth of various algae. Further, selective control of algae was shown without harming existing aquatic plants.
  • Mondo grass, Water Onion and Cabomba were obtained from a local aquarium store and planted in three 2.5L fish tanks. Each tank was treated as follows:
  • Tanks 1, 2 and 3 were monitored for 3 weeks. The results are shown in Table 7 below: Table 7 Description after 3 weeks Tank 1 No visible plant damage was observed. Algae was controlled, Tank 2 Most of the plants were dead. Tank 3 No visible plant damage was observed.
  • a pool of agricultural waste runoff has algae growing throughout the water body of the pool.
  • the algae is unsightly and unattractive.
  • a predetermined effective amount of thaxtomin A is added to the pool to kill the algae.
  • the algae is expected to die and the pool is expected to be cleaner.
  • a child owns an aquarium including tropical fish.
  • the aquarium becomes contaminated with algae which are visible as a scum on the glass walls of the aquarium.
  • One or more thaxtomins is added to the aquarium to kill the algae.
  • the walls are expected to clear and the algae contamination is expected to subside.
  • An aquarium susceptible to algae growth is prophylactically treated by adding thaxtomins to the tank. Algae contamination is expected to be prevented.
  • Thaxtomin and thaxtomin compositions in accordance with the present disclosure are applied to the siding and deck planks of a house. Algae contamination is expected to be prevented for up to 2-6 months.
  • Thaxtomin and thaxtomin compositions in accordance with the present disclosure are applied to fish farm waters. Algae contamination is expected to be prevented for up to 2-6 months.
  • Thaxtomin in accordance with the present disclosure is added to a water carrier solution to a concentration of 100 ppm.
  • the solution is sprayed onto soiled algae bioreactors used to create algae for the production of biofuel.
  • the bioreactors are expected to become clean and unsoiled.
  • Thaxtomin in accordance with the present disclosure is applied to a lawn or golf green which is contaminated with algae growth.
  • the lawn or green is expected to lose the algae contamination, with little or no harm to existing grasses.

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Claims (11)

  1. Procédé d'inhibition de la croissance d'algues comprenant la mise en contact d'algues avec une quantité efficace d'une ou plusieurs thaxtomines.
  2. Procédé selon la revendication 1, dans lequel la ou les thaxtomines incluent des composés choisis dans le groupe constitué de thaxtomine A, thaxtomine B, thaxtomine D, et des combinaisons de celles-ci.
  3. Procédé selon la revendication 1, dans lequel la ou les thaxtomines comprennent la thaxtomine A.
  4. Procédé selon la revendication 1, dans lequel l'algue est dans un environnement liquide.
  5. Procédé selon la revendication 4, dans lequel l'environnement liquide est l'eau.
  6. Procédé selon la revendication 4, dans lequel l'environnement liquide est un réservoir, un étang, une rizière, un lac, un ruisseau, une rivière, un océan, un estuaire, une eau douce d'aquarium, une eau salée d'aquarium, un réservoir pour l'aquaculture commerciale, une citerne pour l'aquaculture commerciale, un étang ornemental, un jardin d'eau, et une combinaison de ceux-ci.
  7. Procédé selon la revendication 1, dans lequel l'algue est dans un sol ou un environnement boueux.
  8. Procédé selon la revendication 1, dans lequel la quantité efficace est une quantité où la concentration appliquée est de 0,5 ppm à 100 ppm.
  9. Procédé selon l'une quelconque des revendications précédentes, dans lequel la ou les thaxtomines ont la composition suivante :
    Figure imgb0005
     où R1 est un méthyl ou H, R2 est un hydroxy ou H, R3 est un méthyl ou H, R4 est un hydroxy ou H, R5 est un hydroxy ou H, R6 est un hydroxy ou H, et des combinaisons de ceux-ci.
  10. Procédé selon la revendication 9, dans lequel R1 est un méthyl, R2 est un hydroxy, R3 est un méthyl, R4 est H, R5 est un hydroxy, R6 est H.
  11. Procédé selon l'une quelconque des revendications précédentes, dans lequel la thaxtomine est mélangée avec un support pour former une solution ayant de la thaxtomine à une concentration de 0,05 ppm à 500 ppm.
EP08745224A 2007-04-09 2008-04-07 Procedes de lutte contre les algues a l'aide de thaxtomine et compositions de thaxtomine Not-in-force EP2178374B1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP12177744.5A EP2520167B1 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine
EP14168205.4A EP2792243B1 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91072307P 2007-04-09 2007-04-09
PCT/US2008/059550 WO2008124675A2 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine

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EP14168205.4A Division EP2792243B1 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine
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EP14168205.4A Not-in-force EP2792243B1 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine
EP12177744.5A Not-in-force EP2520167B1 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine
EP08745224A Not-in-force EP2178374B1 (fr) 2007-04-09 2008-04-07 Procedes de lutte contre les algues a l'aide de thaxtomine et compositions de thaxtomine

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EP12177744.5A Not-in-force EP2520167B1 (fr) 2007-04-09 2008-04-07 Procédés de lutte contre les algues à l'aide de thaxtomine et compositions de thaxtomine

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EP (3) EP2792243B1 (fr)
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CN103749463B (zh) 2015-09-09
ES2488857T3 (es) 2014-08-29
WO2008124675A3 (fr) 2009-09-24
US20080248956A1 (en) 2008-10-09
EP2520167A1 (fr) 2012-11-07
WO2008124675A2 (fr) 2008-10-16
CN101677561B (zh) 2014-03-12
ES2593207T3 (es) 2016-12-07
EP2520167B1 (fr) 2014-05-21
EP2792243A1 (fr) 2014-10-22
EP2792243B1 (fr) 2016-07-06
CN103749463A (zh) 2014-04-30
CN101677561A (zh) 2010-03-24
US7989393B2 (en) 2011-08-02
EP2178374A2 (fr) 2010-04-28
ES2401915T3 (es) 2013-04-25

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